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  • One-pot synthesis of 1,3-disubstituted allenes from 1-alkynes, aldehydes, and morpholine.

One-pot synthesis of 1,3-disubstituted allenes from 1-alkynes, aldehydes, and morpholine.

Journal of the American Chemical Society (2010-01-28)
Jinqiang Kuang, Shengming Ma
ABSTRACT

ZnI(2) has been identified as the catalyst for the one-step synthesis of allenes from terminal alkynes and aldehydes with morpholine as the base in toluene. The reaction is believed to proceed via the intermediacy of propargylic amines, which was converted to allenes by a sequential hydride transfer and beta-elimination process. The reaction is applicable for both aromatic and aliphatic aldehydes. Functionalities such as halide, hydroxyl, or amine may be tolerated.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Morpholine, ACS reagent, ≥99.0%
Sigma-Aldrich
Zinc iodide, anhydrous, powder, 99.999% trace metals basis
Sigma-Aldrich
Zinc iodide, ≥98%
Sigma-Aldrich
Zinc iodide, purum p.a., ≥98.0% (AT)
Sigma-Aldrich
Zinc iodide, ≥99.99% trace metals basis